Green synthesis of MIL-100(Fe) derivatives and revealing their structure-activity relationship for 2,4-dichlorophenol photodegradation

MIL-100(Fe), a kind of iron-based metal-organic framework materials (MOFs), can be synthesized at room temperature or hydrothermal conditions, which are promising precursor materials for preparing photocatalysts to degrade some recalcitrant chlorophenols in industrial wastewater. However, the relationship between the structural characterization of MIL-100(Fe) derivatives and their photodegradation behavior of chlorophenol pollutants is still unclear. Thus, in this work, a porous Z-scheme α-Fe2O3/MIL-100(Fe) composite was successfully fabricated via partial-pyrolysis of MIL-100(Fe) precursor synthesized through green synthesis route, which was further used for degrading high-concentration of 2,4-dichlorophenol under visible-light illumination (λ > 420 nm). The effects of synthesis route and pyrolysis temperature of MIL-100(Fe) on the degradation efficiencies of as-derived materials for 2,4-dichlorophenol were investigated. The structure-activity relationship was illuminated in detail. Otherwise, the influence of several process factors, i.e., initial concentration and pH of the 2,4-dichlorophenol solution, catalyst dosage on the degradation efficiency of 2,4-dichlorophenol has also been performed. The removal efficiency of 2,4-dichlorophenol with the initial concentration of 100 mg L-1 reached up to 87.65% under optimized conditions. Lastly, the possible mechanism was explored based on trapping experiments and some other characterization results. The study in this paper not only exhibited new insight into the modified α-Fe2O3 material with high photocatalytic activity but also provided a promising method for treating wastewater containing 2,4-dichlorophenol or other similar organic pollutants.